Canonical Allele Identifier: CA468407450

Gene: CUBN

Linked Data

• gnomAD v4: 10-16828826-G-C
• MyVariant Identifiers: chr10:g.16870825G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828826G>C , CM000672.2:g.16828826G>C	GRCh38
NC_000010.10:g.16870825G>C , CM000672.1:g.16870825G>C	GRCh37
NC_000010.9:g.16910831G>C	NCBI36
NG_008967.1:g.305992C>G , LRG_540:g.305992C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10743C>G MANE Select	ENSP00000367064.4:p.Ser3581=
ENST00000377833.8:c.10743C>G	ENSP00000367064.4:p.Ser3581=
NM_001081.3:c.10743C>G , LRG_540t1:c.10743C>G	NP_001072.2:p.Ser3581=
XM_011519709.1:c.6729C>G	XP_011518011.1:p.Ser2243=
XM_011519710.1:c.6705C>G	XP_011518012.1:p.Ser2235=
XM_011519711.1:c.6585C>G	XP_011518013.1:p.Ser2195=
XM_011519709.2:c.6729C>G	XP_011518011.1:p.Ser2243=
XM_011519710.2:c.6705C>G	XP_011518012.1:p.Ser2235=
XM_011519711.3:c.6585C>G	XP_011518013.1:p.Ser2195=
NM_001081.4:c.10743C>G MANE Select	NP_001072.2:p.Ser3581=